# FDA Inspection 969545 - Randox Laboratories, Limited - April 28, 2016

Source: https://www.keypedia.com/records/fda_inspections/randox-laboratories-limited/441a0146-d9ca-43ce-a728-7b45707e020d
Source feed: FDA_Inspections

> FDA Inspection 969545 for Randox Laboratories, Limited on April 28, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 969545
- Company Name: Randox Laboratories, Limited
- Inspection Date: 2016-04-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 969514 - 2016-04-28](https://www.keypedia.com/records/fda_inspections/randox-laboratories-limited/b853afcb-4867-4185-a251-15dda3910551)
- [FDA Inspection 817316 - 2012-11-29](https://www.keypedia.com/records/fda_inspections/randox-laboratories-limited/ba313df0-02c5-48c9-a6f4-682bb787683b)
- [FDA Inspection 817316 - 2012-11-29](https://www.keypedia.com/records/fda_inspections/randox-laboratories-limited/2700c5db-03b7-4e01-96c4-9b22dd474d68)

Company: https://www.keypedia.com/companies/randox-laboratories-limited/8a08dce9-5103-4fad-a76a-546f1df5aa53

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
